Far Red/Near-Infrared AIE Dots for Image-Guided Photodynamic Cancer Cell Ablation

被引:106
作者
Feng, Guangxue [1 ]
Wu, Wenbo [1 ,2 ]
Xu, Shidang [1 ]
Liu, Bin [1 ,3 ]
机构
[1] Natl Univ Singapore, Dept Chem & Biomol Engn, 4 Engn Dr 4, Singapore 117585, Singapore
[2] Natl Univ Singapore, Dept Mat Sci & Engn, 7 Engn Dr 1, Singapore 117574, Singapore
[3] Inst Mat Res & Engn, 2 Fusionopolis Way, Singapore 136834, Singapore
基金
新加坡国家研究基金会;
关键词
photodynamic therapy; bioimaging; nanoparticles; aggregation-induced emission; theranostics; AGGREGATION-INDUCED EMISSION; ULTRABRIGHT ORGANIC DOTS; POLYMER NANOPARTICLES; THERAPY; PROBE; BRIGHT; GAP;
D O I
10.1021/acsami.6b06136
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
We report a facile encapsulation approach to realize bright far red/near-infrared (FR/NIR) fluorescence and efficient singlet oxygen COD production of organic fluorogens with aggregation-induced emission (AIEgen) and intramolecular charge transfer (ICT) characteristics for image-guided photodynamic cancer cell ablation. The synthesized AIEgen BTPEAQ possesses donor-acceptor-donor structure, which shows bright fluorescence in solid state. Due to the strong ICT effect, BTPEAQ exhibits poor emission with almost no O-1(2) generation in aqueous solution. Encapsulation of BTPEAQ by DSPE-PEG block copolymer yields polymer-shelled dots, which show enhanced brightness with a fluorescence quantum yield of 3.9% and a O-1(2) quantum yield of 38%. Upon encapsulation by silica, the formed SiO2-shelled dots show much improved fluorescence quantum yield of 12.1% but with no obvious O-1(2) generation. This study clearly demonstrates the importance of encapsulation approach for organic fluorophores, which affects not only the brightness but also the O-1(2) production. After conjugating the polymer-shelled AIE dots with cRGD peptide, the obtained BTPEAQ-cRGD dots show excellent photoablation toward MDA-MB-231 cells with integrin overexpression while keeping control cells intact.
引用
收藏
页码:21193 / 21200
页数:8
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